The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]

Background Cystic fibrosis (CF) is a multiorgan disease affecting the lungs pancreas and gastrointestinal tract. Pulmonary complications are the most common manifestation of the disease. Recent advances in the treatment of pulmonary complications have resulted in substantial improvement in life expe...

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Main Authors: Ao Sasame, Lucy Connolly, Emer Fitzpatrick, Diarmuid Stokes, Billy Bourke, Marion Rowland
Format: Article
Language:English
Published: F1000 Research Ltd 2020-12-01
Series:HRB Open Research
Online Access:https://hrbopenresearch.org/articles/3-44/v3
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spelling doaj-d415bd37eb714dc2b15637efd2033de32021-01-04T17:08:29ZengF1000 Research LtdHRB Open Research2515-48262020-12-01310.12688/hrbopenres.13065.314345The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]Ao Sasame0Lucy Connolly1Emer Fitzpatrick2Diarmuid Stokes3Billy Bourke4Marion Rowland5School of Medicine, University College Dublin, Dublin, IrelandSchool of Medicine, University College Dublin, Dublin, IrelandChildren’s Health Ireland at Crumlin, Dublin, IrelandSchool of Medicine, University College Dublin, Dublin, IrelandSchool of Medicine, University College Dublin, Dublin, IrelandSchool of Medicine, University College Dublin, Dublin, IrelandBackground Cystic fibrosis (CF) is a multiorgan disease affecting the lungs pancreas and gastrointestinal tract. Pulmonary complications are the most common manifestation of the disease. Recent advances in the treatment of pulmonary complications have resulted in substantial improvement in life expectancy. Less than 10% of persons with CF (PWCF) develop liver disease (CFLD). There is conflicting evidence about impact of liver disease on mortality in CF, with evidence suggesting that CFLD contributes to increased mortality in CF, while other studies suggest that the impact on mortality is limited. Understanding the contribution of liver disease to mortality in CF is essential if further improvements in life expectancy are to be achieved. Objective: To document the impact of liver disease on life expectancy for PWCF. Methods: This systematic review will be conducted in compliance with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols (PRISMA-P 2015). PubMed, Medline and Embase will be searched for English language publications (1949-2020). Studies reporting the outcome for CFLD will be included where the definition of CFLD is outlined clearly in a CF population. Studies with and without a comparator will be evaluated. Clinical trials of ursodeoxycholic acid will be excluded as well as organ transplantation outcome studies. We will examine all-cause and specific causes of mortality.We will include transplantation in our estimates of all-cause mortality. The Axis Risk of Bias Tool for Observational Studies will be used to evaluate the quality of studies. We will provide a narrative synthesis of our findings using tabular formats to highlight any impact of liver disease on mortality in CF. Conclusion: It is anticipated that this review will bring clarity to the question of whether CFLD shortens life expectancy in PWCF and stimulate new approaches to the management of CFLD.https://hrbopenresearch.org/articles/3-44/v3
collection DOAJ
language English
format Article
sources DOAJ
author Ao Sasame
Lucy Connolly
Emer Fitzpatrick
Diarmuid Stokes
Billy Bourke
Marion Rowland
spellingShingle Ao Sasame
Lucy Connolly
Emer Fitzpatrick
Diarmuid Stokes
Billy Bourke
Marion Rowland
The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]
HRB Open Research
author_facet Ao Sasame
Lucy Connolly
Emer Fitzpatrick
Diarmuid Stokes
Billy Bourke
Marion Rowland
author_sort Ao Sasame
title The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]
title_short The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]
title_full The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]
title_fullStr The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]
title_full_unstemmed The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]
title_sort impact of liver disease on mortality in cystic fibrosis - a systematic review protocol [version 3; peer review: 2 approved, 2 approved with reservations]
publisher F1000 Research Ltd
series HRB Open Research
issn 2515-4826
publishDate 2020-12-01
description Background Cystic fibrosis (CF) is a multiorgan disease affecting the lungs pancreas and gastrointestinal tract. Pulmonary complications are the most common manifestation of the disease. Recent advances in the treatment of pulmonary complications have resulted in substantial improvement in life expectancy. Less than 10% of persons with CF (PWCF) develop liver disease (CFLD). There is conflicting evidence about impact of liver disease on mortality in CF, with evidence suggesting that CFLD contributes to increased mortality in CF, while other studies suggest that the impact on mortality is limited. Understanding the contribution of liver disease to mortality in CF is essential if further improvements in life expectancy are to be achieved. Objective: To document the impact of liver disease on life expectancy for PWCF. Methods: This systematic review will be conducted in compliance with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols (PRISMA-P 2015). PubMed, Medline and Embase will be searched for English language publications (1949-2020). Studies reporting the outcome for CFLD will be included where the definition of CFLD is outlined clearly in a CF population. Studies with and without a comparator will be evaluated. Clinical trials of ursodeoxycholic acid will be excluded as well as organ transplantation outcome studies. We will examine all-cause and specific causes of mortality.We will include transplantation in our estimates of all-cause mortality. The Axis Risk of Bias Tool for Observational Studies will be used to evaluate the quality of studies. We will provide a narrative synthesis of our findings using tabular formats to highlight any impact of liver disease on mortality in CF. Conclusion: It is anticipated that this review will bring clarity to the question of whether CFLD shortens life expectancy in PWCF and stimulate new approaches to the management of CFLD.
url https://hrbopenresearch.org/articles/3-44/v3
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